Literature DB >> 10545233

Developmental basis of pronephric defects in Xenopus body plan phenotypes.

D W Seufert1, H C Brennan, J DeGuire, E A Jones, P D Vize.   

Abstract

We have used monoclonal antibodies that recognize the pronephric tubules or pronephric duct to explore the induction of the embryonic kidney in developing Xenopus embryos. Morphogenesis of the pronephros was examined in UV-ventralized and lithium-dorsalized embryos. We find that the pronephric tubules are present in all but the strongest UV-induced phenotypes, but absent from relatively moderate lithium phenotypes. Interestingly the pronephric duct, which develops from the ventroposterior portion of the pronephric anlage, is missing from more of the mild UV phenotypes than are pronephric tubules. The loss of the capacity to form pronephroi in UV-ventralized embryos is caused by the loss of tissues capable of inducing the pronephric mesoderm, as marginal zone explants from ventralized embryos are still competent to respond to pronephric-inductive signals. Explant recombination experiments indicate that the tissue responsible for both the loss of pronephroi in UV-ventralized embryos and the induction of pronephroi during normal development is the anterior somites. The absence of pronephroi in relatively mild lithium phenotypes has a developmental basis different from that of the UV phenotype, as explants from lithium-treated embryos are effective inducers of pronephroi in recombinants with competent mesoderm, even though they themselves do not form pronephroi in isolation. Together these data indicate that dorsal tissues, especially the anterior somites, are responsible for the establishment of the intermediate mesoderm and the induction of the embryonic kidneys and that even mild dorsalization destroys the capacity to form cells competent to receive this signal. Copyright 1999 Academic Press.

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Year:  1999        PMID: 10545233     DOI: 10.1006/dbio.1999.9476

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  12 in total

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Journal:  Dev Cell       Date:  2010-05-18       Impact factor: 12.270

4.  Requirement of Wnt/beta-catenin signaling in pronephric kidney development.

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6.  Normal levels of p27 are necessary for somite segmentation and determining pronephric organ size.

Authors:  Richard W Naylor; Robert J Collins; Anna Philpott; Elizabeth A Jones
Journal:  Organogenesis       Date:  2009-10       Impact factor: 2.500

7.  Chordin affects pronephros development in Xenopus embryos by anteriorizing presomitic mesoderm.

Authors:  Tracy Mitchell; Elizabeth A Jones; Daniel L Weeks; Michael D Sheets
Journal:  Dev Dyn       Date:  2007-01       Impact factor: 3.780

8.  The nephrogenic potential of the transcription factors osr1, osr2, hnf1b, lhx1 and pax8 assessed in Xenopus animal caps.

Authors:  Christiane Drews; Sabine Senkel; Gerhart U Ryffel
Journal:  BMC Dev Biol       Date:  2011-01-31       Impact factor: 1.978

9.  Lhx1 is required for specification of the renal progenitor cell field.

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10.  The Lhx1-Ldb1 complex interacts with Furry to regulate microRNA expression during pronephric kidney development.

Authors:  Eugenel B Espiritu; Amanda E Crunk; Abha Bais; Daniel Hochbaum; Ailen S Cervino; Yu Leng Phua; Michael B Butterworth; Toshiyasu Goto; Jacqueline Ho; Neil A Hukriede; M Cecilia Cirio
Journal:  Sci Rep       Date:  2018-10-30       Impact factor: 4.379

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